| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:49278031-49278278 | Rare:67 | ||||
| chr20:49812772-49812920 | Common:2; Rare:41 | ||||
| chr20:49915496-49915583 | Common:3; Rare:25 | ||||
| chr20:50153639-50153928 | Common:2; Rare:116 | ||||
| chr20:50958461-50958857 | Common:1; Rare:148; Clinvar:4; Clinvar (benign):4 | ||||
| chr20:51562773-51563002 | Common:3; Rare:45 | ||||
| chr20:53593797-53593924 | Common:1; Rare:50 | ||||
| chr20:56392153-56392687 | Common:6; Rare:143 | ||||
| chr20:56468536-56468710 | Rare:77 | ||||
| chr20:58651064-58651327 | Common:2; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:59042711-59043044 | Common:1; Rare:121 | ||||
| chr20:59940241-59940481 | Rare:96 | ||||
| chr20:62143238-62143807 | Common:8; Rare:230 | ||||
| chr20:62182954-62183050 | Rare:24 | ||||
| chr20:62310701-62311009 | Rare:127; Clinvar (pathogenic):1 |